Boc-2-Methoxy-L-Phenylalanine CAS#: 143415-63-8

Boc-2-Methoxy-L-Phenylalanine Basic information

Product Name:

Boc-2-Methoxy-L-Phenylalanine

Synonyms:

Boc-2-Methoxy-L-Phenylalanine
Boc-L-Phe(2-OMe)-OH
(Tert-Butoxy)Carbonyl 2-Methoxy-L-Phenylalanine
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-methoxyphenyl)propanoic acid
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methoxy-
Boc-2-methoxy-L-phenylalanine 97%
(S)-2-TERT-BUTHOXYCARBONYLAMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID
(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid

CAS:

143415-63-8

MF:

C15H21NO5

MW:

295.33

Mol File:

Mol File

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Boc-2-Methoxy-L-Phenylalanine Chemical Properties

Melting point:: 157°C
storage temp.: 2-8°C
form: powder
color: White to off-white
Major Application: peptide synthesis
InChI: 1S/C15H21NO5/c1-15(2,3)21-14(19)16-11(13(17)18)9-10-7-5-6-8-12(10)20-4/h5-8,11H,9H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1
InChIKey: QMHKMTAKTUUKEK-NSHDSACASA-N
SMILES: OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O

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Safety Information

WGK Germany: WGK 3
Storage Class: 11 - Combustible Solids

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Boc-2-Methoxy-L-Phenylalanine Usage And Synthesis

Uses

Unnatural amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).

reaction suitability

reaction type: Boc solid-phase peptide synthesis
reagent type: ligand
reaction type: C-H Activation

Boc-2-Methoxy-L-PhenylalanineSupplier

Shanghai Hanhong Scientific Co.,Ltd.

Tel: 021-54306202 13764082696
Email: info@hanhongsci.com

SINO High Goal Chemical Technology Co., Ltd.

Tel: 021-57646680 18306277365
Email: sunkai@chembiobanksh.com

Amatek Scientific Co. Ltd.

Tel: 0512-56316828 4008675858
Email: sales@amateksci.com

LABTER PHARMATECH(BEIJING) CO.,LTD

Tel: 010-56330744 18310155299
Email: sales@labter.com.cn

Sigma-Aldrich

Tel: 021-61415566 800-8193336
Email: orderCN@merckgroup.com

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